Nexplanon® Implant for Clinics
$350.99
Description
What Nexplanon Is and How It Works
Nexplanon® is a single-rod, subdermal contraceptive implant designed for long-acting, reversible contraception in professional care settings. Licensed teams integrate this implantable device into women’s health and family planning workflows. Our catalog supports streamlined procurement through US distribution. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.
The small, thin, flexible rod contains a synthetic progestin that is released at a controlled rate after placement. It is inserted beneath the skin of the upper arm using a sterile, preloaded applicator operated by trained staff. The technique follows aseptic standards and established clinic protocols for device verification, placement, and post-procedure checks.
The Nexplanon implant supports programmatic contraception services with predictable scheduling, standardized supply use, and clear device accountability in multi-provider environments.
Professional Applications
Clinics incorporate this implant into comprehensive contraception programs, including routine consults, same‑day procedures when appropriate, and scheduled removals. It fits women’s health pathways that prioritize continuity, adherence, and lower visit burden compared with short-interval methods. Teams often coordinate counseling, consent, insertion, and follow-up as a single, well-documented care episode.
It can sit alongside other options within Contraceptives and broader Family Planning protocols, supported by standard screening and documentation policies. Gynecology services may align implant visits with cervical screening, STI testing, or other preventive care where appropriate. See also our Gynecology and Women’s Health categories for related lines.
Training and competency-based credentialing remain essential for Nexplanon insertion and removal. Supervising clinicians can standardize room setup, sterile technique, and device verification steps to support consistent outcomes across practitioners.
Key Features
- Single-rod implant: small, thin, flexible polymer rod.
- Progestin-only composition: steady hormone release profile.
- Subdermal route: upper arm placement by trained personnel.
- Integrated applicator: sterile, single-use, preloaded device.
- Lot and expiry clarity: traceability via labeled packaging.
- Shelf-stable handling: store as directed on the label.
- Nexplanon device: long-acting option that suits scheduled workflows.
Benefits in Practice
This product can streamline scheduling, since one in-office procedure generally initiates a multi-year method. Fewer refill visits can improve operational efficiency for teams balancing high appointment demand. The preloaded applicator reduces setup time compared with multi-component kits, and supports consistent technique across providers after training.
Inventory planning can be aligned to projected procedure volume. Clinics may pre-book removal and replacement windows to maintain continuity of care. For established patients, staff can pre-authorize insurance where appropriate, prepare instruments, and stage sterile drapes to shorten room turnover. Practices that routinely manage replacing nexplanon can template consent, device verification, and follow-up notes for documentation consistency. See implant options across Implants for inventory planning.
Composition & Ingredients
Active ingredient: etonogestrel. The implant contains a total drug load that is released gradually following insertion. This progestin-only design supports long-acting use when placed correctly.
Each unit is an etonogestrel implant 68 mg. Excipients and detailed component materials are described in the manufacturer’s labeling and device instructions. Review current labeling before use to confirm materials, contraindications, and procedural guidance.
Packaging & Supply
Supplied as a single implant in a sterile, preloaded applicator to support one procedure per unit. The primary carton and device labeling provide lot and expiration details for traceability. Strength: 68 mg (per implant). Pack configuration: 1 implant per applicator.
Product identifier (clinic reference): SKU 82298. The Nexplanon 68 mg implant packaging is intended for professional use and should remain sealed until the procedure. Dispose of the applicator after use according to sharps and device disposal standards.
Ordering & Logistics
Create or verify a professional account to view contract tiers and request allocation. Once approved, sign in to see purchase options aligned to your credentialing and formulary permissions. Our team supports routine replenishment, shipment scheduling, and documentation requests for audits or supplier validations.
For integrated procurement across multiple lines, you can combine women’s health, contraceptive devices, and pharmaceuticals under one invoice. Explore Contraceptives or expand your formulary with adjacent therapies, such as Cardiometabolic Care, to consolidate supply workflows under one account.
Comparable Products
Clinics evaluating long-acting contraception often consider implants alongside other hormonal options. For emergency protocols and counseling materials, see Ella Overview. Teams designing comprehensive contraception services may also review our Contraceptives category and education on Hormonal Injections to support staff training and patient discussions.
Pricing & Access
Sign in to view contract and volume pricing. Tiered structures may be available for clinics with consolidated purchasing, higher monthly usage, or multi-site networks. Your account manager can assist with allocation requests, documentation, and vendor forms as needed for your credentialing workflow.
Availability & Substitutions
Supply can vary based on manufacturer production, distribution windows, and regional allocations. If a specific carton configuration or lot timing is temporarily constrained, confirm acceptable substitutes with your clinical team before placing a request. Your account manager can help align order timing with scheduled clinics, especially for high-volume insertion days.
Authoritative Sources
Manufacturer Information – official product information, device instructions, and professional resources.
FDA Prescribing Information – labeling, contraindications, warnings, and adverse reactions.
MedlinePlus: Etonogestrel Implant – patient education and class overview.
Some users may experience irregular bleeding, headache, weight change, acne, breast tenderness, or mood changes. Rare but serious events can include thromboembolic events, stroke, myocardial infarction, liver tumors, and ectopic pregnancy. Review full labeling for comprehensive safety information and counseling points.
Sign in to request allocation and schedule shipments; we support temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
Who is qualified to insert and remove the implant?
Insertion and removal are performed by trained, licensed clinicians per local regulations and the manufacturer’s instructions. Many clinics designate credentialed providers and maintain competency checklists, in-service training, and periodic skills refreshers. A standardized room setup, sterile field, and device verification process help ensure consistent technique. Supervising staff should also maintain protocols for counseling, consent, post-procedure checks, and documentation, including lot and expiration capture in the medical record.
How long is the implant intended to provide contraception?
The device is designed as a long-acting, reversible method with multi‑year duration as specified in current labeling. Actual duration should follow the manufacturer’s guidance and professional society recommendations. Teams often schedule reminders for removal or replacement well in advance to maintain continuity of care. Always refer to the latest product literature before counseling on duration or timing for follow‑up appointments.
What are the typical adverse effects to discuss during counseling?
Commonly reported effects include irregular bleeding patterns, headache, acne, weight change, breast tenderness, and mood changes. Rare but serious risks may include blood clots, stroke, myocardial infarction, liver tumors, and ectopic pregnancy. Counseling should reference current labeling and consider patient-specific factors and contraindications. Encourage reporting of new or concerning symptoms and ensure clear instructions for when to seek medical attention.
What materials and components are included with each unit?
Each unit contains a single flexible rod with a total etonogestrel drug load and a sterile, single-use applicator. The primary carton and device labeling display lot and expiration details for traceability. Review the current manufacturer instructions for a complete list of materials, device identifiers, and any accessory components that may be included or required for the procedure.
How should clinics plan for removal and potential replacement?
Plan removal appointments ahead of the labeled duration and coordinate staffing for same-day replacement when indicated. Maintain a standardized kit with sterile drapes, local anesthetic per policy, and instruments for removal. Pre-verify device availability, and prepare documentation templates for counseling, consent, device verification, and post-procedure instructions to streamline throughput and maintain consistent records across providers.
What storage conditions apply to the implant?
Follow the current product labeling for storage conditions. The implant is generally managed under standard room-temperature conditions in secure medication storage, away from excessive heat, light, and moisture. Do not open the sterile packaging until the procedure. Dispose of the applicator as sharps after use and document lot and expiration in the patient record or inventory system.
What documentation is recommended for traceability and quality control?
Capture lot number, expiration date, and device identifiers in the patient’s chart and your inventory log. Many clinics scan labels directly into the EHR and retain carton flaps for reconciliation. Maintain procedure notes covering consent, site verification, insertion or removal details, and any post-procedure observations. Consistent documentation supports internal quality assurance and simplifies product or lot queries if needed.
Specifications
- Main Ingredient: Etonogestrel
- Manufacturer: Merck & Co., Inc.
- Drug Class: Progestin-Only Contraceptive
- Generic Name: Etonogestrel Implant
- Package Contents: 68 mg - 1 Implant
- Storage Requirements: Room Temperature (2℃~25℃)
- Main Usage:
About the Brand
Nexplanon
Here to help
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